Evidence map›Paper›PMID 41572645›Full record

ArticleStatistics in medicine2026

Extended Joinpoint Regression Methodology for Complex Survey Data.

Benmei Liu, Hyune-Ju Kim, Joe Zou, Eric J Feuer, Barry I Graubard

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Article in Statistics in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

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0cells of the map it votes in
3citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

5 authors.

Benmei LiuDivision of Cancer Control and Population Sciences, National Cancer Institute, Bethesda, Maryland, USA.ORCID https://orcid.org/0000-0003-0096-139X
Hyune-Ju KimDepartment of Mathematics, Syracuse University, Syracuse, New York, USA.ORCID https://orcid.org/0000-0003-1750-9201
Joe ZouInformation Management Services, Inc., Calverton, Maryland, USA.
Eric J FeuerDivision of Cancer Control and Population Sciences, National Cancer Institute, Bethesda, Maryland, USA.
Barry I GraubardDivision of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, Maryland, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Joinpoint regression can model trends in time-specific aggregated estimates. These methods have been developed mainly for non-survey data such as cancer registry data, and only recently have been extended to utilize survey data that accounts for complex sample designs resulting in non-zero correlation between the time-specific estimates. This correlation can occur for surveys with data from the same sampled units used across time points, for example, the annual National Health Interview Survey with multistage cluster samples using the same first-stage sampled clusters over consecutive time points. Another issue when modeling aggregated data is that the degrees of freedom for joinpoint analyses of multistage cluster samples are based on the number of time points, not the number of first-stage sampled clusters as used in survey methods. To address this, we propose models of individual-level data that incorporate both the correlation between time points and correct the degrees of freedom due to the sampling design that is needed for accurate inferences. Also, a modified design-based Akaike Information Criterion (M-dAIC) for model selection is proposed to account for complex sample designs. These new methods are empirically compared to existing methods using simulation studies and health survey data examples. The simulation studies indicated that this new individual-level model identified the true number of joinpoints more accurately than the established aggregate-level models for data collected using complex survey designs with moderate to large interclass correlation coefficients (ICC).

Indexed as

Models, StatisticalCluster AnalysisComputer SimulationData Interpretation, StatisticalHealth SurveysHumansRegression Analysiscomplex survey dataindividual‐level modeljoinpoint regressionmodified design‐based AICtrend analysis

Identifiers

PMID41572645
PMCPMC12828251

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.